Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion description "[We therefore suggest that routine germline MEN1 mutation testing of all cases of classical MEN1, familial hyperparathyroidism, and sporadic hyperparathyroidism with one other MEN1 related condition is justified by national testing services.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion evidence source_evidence_literature NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion SIO_000772 15635078 NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion wasDerivedFrom befree-2016 NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion wasGeneratedBy ECO_0000203 NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.
- befree-2016 importedOn "2016-02-19" NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance.